Bladder CancerNCT05462392
Robot-assisted Urological Surgeries Using the MicroHand S Robot
A study testing robot-assisted surgery in people with Bladder Cancer and Prostate Cancer, run by The Affiliated Hospital of Qingdao University at 1 site in China.
Trial summary
A single-blinded, prospective randomized parallel controlled clinical trial is designed and will be conducted from July 2022 to November 2023 (anticipated). One hundred and thirty-six patients (anticipated) with renal cancer or bladder cancer or prostate cancer will be enrolled in this study. Read more about this study
- Who is it for?
- Ages 18 to 80 years
- Conditions the study is for
- Bladder Cancer, Prostate Cancer, Renal Cancer
- What is being tested?
- robot-assisted surgery
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 136 participants
- Where
- 1 siteChina
- Study dates
- 28 Jul 2022to Dec 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 80 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- BMI was 18-30 kg/m2;
- patients that need partial nephrectomy, radical cystectomy, and radical prostatectomy.
- patients that understand the benefits and risks of this test, and are willing to participate and sign the informed consent form
Who cannot join
- Previous abdominal and pelvic surgery history (preoperative evaluation may affect this operation)
- People with serious uncontrolled diseases or acute infections, including but not limited to: Patients with active tuberculosis and HIV antibody positive; Those who are positive for hepatitis B surface antigen (HBsAg) or hepatitis B core antibody (HBcAb) and whose copy number of hepatitis B virus DNA (HBV-DNA) is higher than the lower limit of detection or the range of normal values; Hepatitis C virus (HCV) antibody positive; Treponema pallidum positive patients; Covid-19 positive patients
- Long term use of anticoagulant and antiplatelet drugs (antiplatelet aggregation drugs were stopped less than 1 week before operation), and patients with a history of hemorrhagic diseases or hematopoietic dysfunction or coagulation dysfunction; Serious allergic constitution and suspected or confirmed alcohol, drug or drug addiction; Patients with epilepsy or mental history or cognitive impairment
- Patients with cardiovascular and cerebrovascular diseases, blood system diseases, or poor control of blood glucose and blood pressure, who cannot tolerate anesthesia or increase the risk of surgery according to the evaluation of the researcher
- women in pregnancy or lactation
- Patients who have participated or are participating in clinical research of other drugs, biological agents or medical devices in the past 3 months
- Other conditions that the researcher believes are not suitable to participate in this experiment
Trial locations and contacts
1 site in 1 country.
China1 site, 1 recruiting
- Recruiting
The Affiliated Hospital of Qingdao University
Qingdao, Shandong, 266003
Haitao Niu, PhD, 18661803117, niuht0532@126.com
About this study
Official title: Robot-assisted Urological Surgeries Using the MicroHand S Robot: a Prospective, Single Blind, Randomized Controlled Trial
A single-blinded, prospective randomized parallel controlled clinical trial is designed and will be conducted from July 2022 to November 2023 (anticipated). One hundred and thirty-six patients (anticipated) with renal cancer or bladder cancer or prostate cancer will be enrolled in this study. Those patients will be enrolled by two hospital centers and the patients will be randomly divided into the Micro Hand S surgical robot group and the da Vinci surgical robot group. Robot-assisted partial nephrectomy, radical cystectomy, and radical prostatectomy will be conducted using the Micro Hand S robot or the da Vinci robot. The success rate of operation, assembly time, operation time, intraoperative hemorrhage, continence rate (if applicable), postoperative pain, comprehensive complication index, resident time and surgeon satisfaction were recorded. The aim of the study is to determine whether the newly developed Chinese Micro Hand S surgical robot results in non-inferiority outcomes in urological surgeries compared with the prevalent da Vinci robot.
Read the detailed description
Objective: To determine whether the newly developed Chinese Micro Hand S surgical robot results in non-inferiority outcomes in partial nephrectomy, radical cystectomy, and radical prostatectomy, compared with the prevalent da Vinci robot.
Design: A single-blinded, prospective randomized parallel controlled clinical trial will be conducted from July 2022 to November 2023 (anticipated). One hundred and thirty-six patients (anticipated) with renal cancer or bladder cancer or prostate cancer will be enrolled in this study. Those patients will be enrolled by two hospital centers and the patients will be randomly divided into the Micro Hand S surgical robot group and the da Vinci surgical robot group.
Interventions: Robot-assisted urological surgeries, such as partial nephrectomy, radical cystectomy, and radical prostatectomy will be conducted using the Micro Hand S robot or the da Vinci robot.
Main measures: The main outcome was the success rate of operation. Surgical success was defined as that the surgical procedures were completed by the experimental or control product without transferring to non-robotic surgery. Secondary outcomes included intra- and post-operative complications, comprehensive complication index, assembly time, operation time, intraoperative hemorrhage, postoperative pain, resident time, surgeon satisfaction, incidence of adverse events, instrument malfunction, vital signs, routine blood test, hepatic and liver function.
Background:
Prostate cancer is a common disease of elderly male. With the continuous growth of life expectancy, the change of diet structure and the improvement of diagnostic technology, the incidence rate of prostate cancer has increased in recent years. Radical prostatectomy can be performed for cancer confined within the prostate capsule, which is also the best treatment for prostate cancer. At present, the commonly used surgical methods include traditional open prostatectomy, laparoscopic prostatectomy, and robot-assisted prostatectomy.
Minimally invasive surgery has always been the unremitting pursuit of surgeons. In the past decade, da Vinci robot system has expanded rapidly in China, especially in some fields of Urology, showing great advantages. In July 2000, da Vinci robotic surgery system was approved by FDA for clinical surgery. In July 2001, binder and others completed the world's first da Vinci robotic surgery system assisted laparoscopic radical prostatectomy. Since then, da Vinci robotic surgery has been widely used in clinical surgery worldwide, such as Urology, general surgery, cardiothoracic surgery, obstetrics and Gynecology, pediatric surgery, etc. In recent ten years, da Vinci robotic surgery in China has developed rapidly, and the number of urological surgery cases is increasing rapidly. It is widely used in radical prostatectomy, partial nephrectomy, radical cystectomy, pyeloplasty, adrenalectomy and other urological surgery. This is mainly due to the unique anatomical structure of Urology, which enables da Vinci system to take its advantages such as 3D high-definition vision, precise cutting and separation, intracavitary suture technology, and short learning curve.
The special anatomical position of the prostate and the surrounding anatomical structure determine the difficulty of the operation. In terms of learning curve, it needs 50-100 cases for laparoscopic surgery to pass the learning curve, and it needs 10-20 cases for da Vinci robotic surgery system to pass the learning curve; In terms of visual field, the anatomy of robot assisted surgery is clearer, which is conducive to the protection of urethral membrane and neurovascular bundle, and sexual function, and the "double construction" of anatomy and function. In addition, it also has the characteristics of less bleeding and complications, rapid postoperative recovery, short hospital stay, and can achieve the same or better oncological and functional results.
In nephrectomy or partial nephrectomy, compared with laparoscopic surgery, the learning curve is greatly shortened; By providing high-resolution and three-dimensional images, magnifying the images can make the surgical field clearer; Moreover, the da Vinci robotic surgery system has seven degrees of freedom, which can simulate the movement of the hand, so that the surgeon can better complete the incision, fine suture and reconstruction, zoom action, tremor filtering, which can alleviate the hand fatigue of the surgeon, greatly increase the safety of hand surgery, reduce the time of renal warm ischemia, and maximize the protection of renal function.
In conclusion, when performing radical prostatectomy, radical cystectomy or partial nephrectomy using robot surgery system, it has certain advantages compared with laparoscopic surgery, and it also needs to record its related complications, especially electrical machinery related complications.
Method:
The study was designed as a single-blind prospective randomized clinical trial since it is inevitable for the surgeon to know what kind of robot to use during the operation. After obtaining the approval of the Ethics Review Committee and other relevant institutions, a total of 136 patients will be included in this study from from July 2022 to November 2023 (anticipated). Those patients will be enrolled by two hospital centers and the patients will be randomly divided into the Micro Hand S surgical robot group and the da Vinci surgical robot group. All enrolled patients were fully informed and signed the informed consent. Patients were randomly assigned to each group in a 1:1 ratio, and information of the grouping and intervention measures were not available to patients. Patients of each group were matched for age, sex, body mass index (BMI), and complications to reduce confounding intervention factors. Robot-assisted partial nephrectomy, radical cystectomy, and radical prostatectomy will be conducted using the Micro Hand S robot or the da Vinci robot. The success rate of operation, assembly time, operation time, intraoperative hemorrhage, continence rate (if applicable), postoperative pain, comprehensive complication index, resident time and surgeon satisfaction were recorded.
Robot-assisted partial nephrectomy, radical cystectomy, and radical prostatectomy will be conducted using the Micro Hand S robot or the da Vinci robot. During the operation, the assembly time, intraoperative blood loss, operation time, operation success rate, and the adjacent organ and vascular injury caused by the failure of the tested system were recorded. Pain score was analyzed 24±2 hours after the surgery. The vital signs (temperature, pulse, respiration, blood pressure) were measured on the 3rd day postoperatively. Meanwhile, the routine blood test (red blood cells, white blood cells and neutrophils, platelet, hemoglobin), liver and renal function (ALT, AST, TP, ALB, GLU, TBIL, BUN, and CREA), the electrolyte (K, Na, Cl, Ca), blood sugar, and color ultrasound of liver, gallbladder, pancreas and spleen were checked. Operating surgeons filled in the satisfaction questionnaire postoperatively. Furthermore, the patients' postoperative condition changes, postoperative medication, postoperative complications, and resident time were also recorded. All the patients were followed up by telephone at 30±5 days postoperatively to evaluate the incidence of adverse events.
- Conditions
- Bladder Cancer, Prostate Cancer, Renal Cancer
- Being tested
- robot-assisted surgery
- Medical subject headings
- Urinary Bladder Neoplasms, Prostatic Neoplasms, Kidney Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
robot-assisted surgeryDevice
urological surgeries, such as partial nephrectomy, radical cystectomy, and radical prostatectomy was performed for patients using the Micro Hand S robot group.
robot-assisted surgeryDevice
urological surgeries, such as partial nephrectomy, radical cystectomy, and radical prostatectomy was performed for patients using the da Vinci robot group
| Study group | Role | What they receive |
|---|---|---|
| the Micro Hand S robot group | Experimental | 68 patients were randomly allocated in the Micro Hand S robot group and partial nephrectomy, radical cystectomy, and radical prostatectomy will be performed using the Micro Hand S robot. Receives: Device: robot-assisted surgery |
| the da Vinci robot group | Other | 68 patients were randomly allocated in the da Vinci robot group and partial nephrectomy, radical cystectomy, and radical prostatectomy will be performed using the da Vinci robot. Receives: Device: robot-assisted surgery |
What is being measured
The primary outcome is the main question the study is designed to answer.
Success rate of the surgery
the proportion of patients with successful operation in all participating patients in the experimental or control group
Measured: after the study is completed, up to 18 months
Secondary outcomes (1)
assembly time
The assembly time extends from the time the robot starts to the time the trocar is connected to the robot arm.
Measured: after the robot is assembled, all data will be collected within 18 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Jul 2022
- Study start28 Jul 2022
- Primary completionNov 2023 (estimated)
- Study completionDec 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Bladder CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- randomized controlled trial
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 136 participants (estimated)
Sponsor and investigators
- Lead sponsor
- The Affiliated Hospital of Qingdao University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05462392
- Sponsor's protocol ID
- NKJSSQXCKXT02-WG
- Status last verified
- Aug 2023
- First submitted
- 14 Jul 2022
- Last updated
- 2 Aug 2023
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Yuan H, Wang Y, Ji Y. Robotic-assisted Urological Minimally Invasive Cancer Surgeries using the MicroHand S Surgical Robot System. Arch Esp Urol. 2026 Apr;79(3):484-494. doi: 10.56434/j.arch.esp.urol.20267903.57.
PubMed 42104703
Study at a glance
From the registry record, last updated by the sponsor on 2 Aug 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Robot-assisted Urological Surgeries Using the MicroHand S Robot: a Prospective, Single Blind, Randomized Controlled Trial
- ClinicalTrials.gov ID
- NCT05462392
- Acronym / sponsor ID
- NKJSSQXCKXT02-WG
- Conditions
- Bladder Cancer, Prostate Cancer, Renal Cancer
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 136 participants (estimated)
- Lead sponsor
- The Affiliated Hospital of Qingdao UniversityUniversity, hospital or other
- Study start
- 28 Jul 2022 (actual)
- Primary completion
- Nov 2023 (estimated)
- Study completion
- Dec 2023 (estimated)
- First posted
- 18 Jul 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
A single-blinded, prospective randomized parallel controlled clinical trial is designed and will be conducted from July 2022 to November 2023 (anticipated). One hundred and thirty-six patients (anticipated) with renal cancer or bladder cancer or prostate cancer will be enrolled in this study. Those patients will be enrolled by two hospital centers and the patients will be randomly divided into the Micro Hand S surgical robot group and the da Vinci surgical robot group. Robot-assisted partial nephrectomy, radical cystectomy, and radical prostatectomy will be conducted using the Micro Hand S robot or the da Vinci robot. The success rate of operation, assembly time, operation time, intraoperative hemorrhage, continence rate (if applicable), postoperative pain, comprehensive complication index, resident time and surgeon satisfaction were recorded. The aim of the study is to determine whether the newly developed Chinese Micro Hand S surgical robot results in non-inferiority outcomes in urological surgeries compared with the prevalent da Vinci robot.
Detailed description
Objective: To determine whether the newly developed Chinese Micro Hand S surgical robot results in non-inferiority outcomes in partial nephrectomy, radical cystectomy, and radical prostatectomy, compared with the prevalent da Vinci robot.
Design: A single-blinded, prospective randomized parallel controlled clinical trial will be conducted from July 2022 to November 2023 (anticipated). One hundred and thirty-six patients (anticipated) with renal cancer or bladder cancer or prostate cancer will be enrolled in this study. Those patients will be enrolled by two hospital centers and the patients will be randomly divided into the Micro Hand S surgical robot group and the da Vinci surgical robot group.
Interventions: Robot-assisted urological surgeries, such as partial nephrectomy, radical cystectomy, and radical prostatectomy will be conducted using the Micro Hand S robot or the da Vinci robot.
Main measures: The main outcome was the success rate of operation. Surgical success was defined as that the surgical procedures were completed by the experimental or control product without transferring to non-robotic surgery. Secondary outcomes included intra- and post-operative complications, comprehensive complication index, assembly time, operation time, intraoperative hemorrhage, postoperative pain, resident time, surgeon satisfaction, incidence of adverse events, instrument malfunction, vital signs, routine blood test, hepatic and liver function.
Background:
Prostate cancer is a common disease of elderly male. With the continuous growth of life expectancy, the change of diet structure and the improvement of diagnostic technology, the incidence rate of prostate cancer has increased in recent years. Radical prostatectomy can be performed for cancer confined within the prostate capsule, which is also the best treatment for prostate cancer. At present, the commonly used surgical methods include traditional open prostatectomy, laparoscopic prostatectomy, and robot-assisted prostatectomy.
Minimally invasive surgery has always been the unremitting pursuit of surgeons. In the past decade, da Vinci robot system has expanded rapidly in China, especially in some fields of Urology, showing great advantages. In July 2000, da Vinci robotic surgery system was approved by FDA for clinical surgery. In July 2001, binder and others completed the world's first da Vinci robotic surgery system assisted laparoscopic radical prostatectomy. Since then, da Vinci robotic surgery has been widely used in clinical surgery worldwide, such as Urology, general surgery, cardiothoracic surgery, obstetrics and Gynecology, pediatric surgery, etc. In recent ten years, da Vinci robotic surgery in China has developed rapidly, and the number of urological surgery cases is increasing rapidly. It is widely used in radical prostatectomy, partial nephrectomy, radical cystectomy, pyeloplasty, adrenalectomy and other urological surgery. This is mainly due to the unique anatomical structure of Urology, which enables da Vinci system to take its advantages such as 3D high-definition vision, precise cutting and separation, intracavitary suture technology, and short learning curve.
The special anatomical position of the prostate and the surrounding anatomical structure determine the difficulty of the operation. In terms of learning curve, it needs 50-100 cases for laparoscopic surgery to pass the learning curve, and it needs 10-20 cases for da Vinci robotic surgery system to pass the learning curve; In terms of visual field, the anatomy of robot assisted surgery is clearer, which is conducive to the protection of urethral membrane and neurovascular bundle, and sexual function, and the "double construction" of anatomy and function. In addition, it also has the characteristics of less bleeding and complications, rapid postoperative recovery, short hospital stay, and can achieve the same or better oncological and functional results.
In nephrectomy or partial nephrectomy, compared with laparoscopic surgery, the learning curve is greatly shortened; By providing high-resolution and three-dimensional images, magnifying the images can make the surgical field clearer; Moreover, the da Vinci robotic surgery system has seven degrees of freedom, which can simulate the movement of the hand, so that the surgeon can better complete the incision, fine suture and reconstruction, zoom action, tremor filtering, which can alleviate the hand fatigue of the surgeon, greatly increase the safety of hand surgery, reduce the time of renal warm ischemia, and maximize the protection of renal function.
In conclusion, when performing radical prostatectomy, radical cystectomy or partial nephrectomy using robot surgery system, it has certain advantages compared with laparoscopic surgery, and it also needs to record its related complications, especially electrical machinery related complications.
Method:
The study was designed as a single-blind prospective randomized clinical trial since it is inevitable for the surgeon to know what kind of robot to use during the operation. After obtaining the approval of the Ethics Review Committee and other relevant institutions, a total of 136 patients will be included in this study from from July 2022 to November 2023 (anticipated). Those patients will be enrolled by two hospital centers and the patients will be randomly divided into the Micro Hand S surgical robot group and the da Vinci surgical robot group. All enrolled patients were fully informed and signed the informed consent. Patients were randomly assigned to each group in a 1:1 ratio, and information of the grouping and intervention measures were not available to patients. Patients of each group were matched for age, sex, body mass index (BMI), and complications to reduce confounding intervention factors. Robot-assisted partial nephrectomy, radical cystectomy, and radical prostatectomy will be conducted using the Micro Hand S robot or the da Vinci robot. The success rate of operation, assembly time, operation time, intraoperative hemorrhage, continence rate (if applicable), postoperative pain, comprehensive complication index, resident time and surgeon satisfaction were recorded.
Robot-assisted partial nephrectomy, radical cystectomy, and radical prostatectomy will be conducted using the Micro Hand S robot or the da Vinci robot. During the operation, the assembly time, intraoperative blood loss, operation time, operation success rate, and the adjacent organ and vascular injury caused by the failure of the tested system were recorded. Pain score was analyzed 24±2 hours after the surgery. The vital signs (temperature, pulse, respiration, blood pressure) were measured on the 3rd day postoperatively. Meanwhile, the routine blood test (red blood cells, white blood cells and neutrophils, platelet, hemoglobin), liver and renal function (ALT, AST, TP, ALB, GLU, TBIL, BUN, and CREA), the electrolyte (K, Na, Cl, Ca), blood sugar, and color ultrasound of liver, gallbladder, pancreas and spleen were checked. Operating surgeons filled in the satisfaction questionnaire postoperatively. Furthermore, the patients' postoperative condition changes, postoperative medication, postoperative complications, and resident time were also recorded. All the patients were followed up by telephone at 30±5 days postoperatively to evaluate the incidence of adverse events.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
- Model description
- randomized controlled trial
| Arm | Type | Receives |
|---|---|---|
| the Micro Hand S robot group | Experimental | Device: robot-assisted surgery68 patients were randomly allocated in the Micro Hand S robot group and partial nephrectomy, radical cystectomy, and radical prostatectomy will be performed using the Micro Hand S robot. |
| the da Vinci robot group | Other | Device: robot-assisted surgery68 patients were randomly allocated in the da Vinci robot group and partial nephrectomy, radical cystectomy, and radical prostatectomy will be performed using the da Vinci robot. |
Who may qualify
- Ages
- 18 to 80 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- BMI was 18-30 kg/m2;
- patients that need partial nephrectomy, radical cystectomy, and radical prostatectomy.
- patients that understand the benefits and risks of this test, and are willing to participate and sign the informed consent form
Key exclusion criteria (7 listed)
- Previous abdominal and pelvic surgery history (preoperative evaluation may affect this operation)
- People with serious uncontrolled diseases or acute infections, including but not limited to: Patients with active tuberculosis and HIV antibody positive; Those who are positive for hepatitis B surface antigen (HBsAg) or hepatitis B core antibody (HBcAb) and whose copy number of hepatitis B virus DNA (HBV-DNA) is higher than the lower limit of detection or the range of normal values; Hepatitis C virus (HCV) antibody positive; Treponema pallidum positive patients; Covid-19 positive patients
- Long term use of anticoagulant and antiplatelet drugs (antiplatelet aggregation drugs were stopped less than 1 week before operation), and patients with a history of hemorrhagic diseases or hematopoietic dysfunction or coagulation dysfunction; Serious allergic constitution and suspected or confirmed alcohol, drug or drug addiction; Patients with epilepsy or mental history or cognitive impairment
- Patients with cardiovascular and cerebrovascular diseases, blood system diseases, or poor control of blood glucose and blood pressure, who cannot tolerate anesthesia or increase the risk of surgery according to the evaluation of the researcher
- women in pregnancy or lactation
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| robot-assisted surgeryurological surgeries, such as partial nephrectomy, radical cystectomy, and radical prostatectomy was performed for patients using the Micro Hand S robot group. | Device | the Micro Hand S robot group |
| robot-assisted surgeryurological surgeries, such as partial nephrectomy, radical cystectomy, and radical prostatectomy was performed for patients using the da Vinci robot group | Device | the da Vinci robot group |
Primary outcome
Success rate of the surgery
Time frame: after the study is completed, up to 18 months
the proportion of patients with successful operation in all participating patients in the experimental or control group
1 secondary outcome
assembly time
Time frame: after the robot is assembled, all data will be collected within 18 months
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Aug 2023.
- Derived from this study: PubMed 42104703Yuan H, Wang Y, Ji Y. Robotic-assisted Urological Minimally Invasive Cancer Surgeries using the MicroHand S Surgical Robot System. Arch Esp Urol. 2026 Apr;79(3):484-494. doi: 10.56434/j.arch.esp.urol.20267903.57.
- Individual participant dataSharing planned: No
Related trials for Bladder Cancer
Active, not recruitingEarly Phase 1
(CLONEVO): Cell cycLe inhbitiON to Target the EVolution of UrOthelial Cancer
Bladder Cancer
Not yet recruitingObservational study
Outcomes for IR and High Risk (HR) Non-muscle Invasive Bladder Cancer (NMIBC) and ctDNA-based Biomarkers for Response and Recurrence in Muscle Invasive Bladder Cancer (MIBC)
NMIBC, MIBC
RecruitingPhase 2/3
Testing the Role of DNA Released From Tumor Cells Into the Blood in Guiding the Use of Immunotherapy After Surgical Removal of the Bladder, Kidney, Ureter, and Urethra for Urothelial Cancer Treatment, MODERN Study
Muscle Invasive Bladder Urothelial Carcinoma, Muscle Invasive Renal Pelvis Urothelial Carcinoma
Active, not recruitingPhase 2
Intravesical Gem/Doce in Patients With NMIBC
Urinary Bladder Cancer
Active, not recruitingPhase 3
Testing the Addition of the Anti-cancer Drug, Cabozantinib, to the Usual Immunotherapy Treatment, Avelumab, in Patients With Metastatic Urothelial Cancer, MAIN-CAV Study
Advanced Bladder Urothelial Carcinoma, Advanced Renal Pelvis Urothelial Carcinoma
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing robot-assisted surgery in people with Bladder Cancer and Prostate Cancer, run by The Affiliated Hospital of Qingdao University at 1 site in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 2 Aug 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Success rate of the surgery (time frame: after the study is completed, up to 18 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05462392, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Aug 2023.